Composition and method for removing metal contaminants

ABSTRACT

A composition comprising a substrate, an organic ion, and a metal binding agent, wherein the substrate comprises a natural clay, a synthetic clay, a natural zeolite, a synthetic zeolite, a polymer resin, lignite, kaolinite, serpentine, illite, chlorite, smectite, montmorillonite, saponite, sepiolite, nontronite, beidellite, hectorite, fuller&#39;s earth, attapulgite, bentonite, analcime, chabazite, heulandite, natrolite, phillipsite, stilbite, diethyl aminoethyl, quaternary aminoethyl, or combinations thereof, wherein the organic ion comprises quaternary amines, imidazolium salts, phosphonium salts, tetra alkyl ammonium, bis-(hydrogenated tallow)-dimethyl-ammonium chloride, bis-(hydrogenated tallow)-benzyl-methyl-ammonium chloride, 4,5-dihydro-1-methyl-2-nortallow-alkyl-1-(2-tallow-amidoethyl)-imidazolium methyl sulfate, 1-ethyl-4,5-dihydro-3-(2-hydroxyethyl)-2-(8-heptadecenyl)-imidazolium ethyl sulfate, or combinations thereof, and wherein the metal-binding agent comprises mercaptan, carboxylic acid, chelating agents, amines, esters, carboxylic acids, alcohols, ethers, aldehydes, ketones, alkenes, alkynes, mercaptans, thiols, tert-dodecanethiol, nonanethiol, octanethiol, n-stearic acid, iso-stearic acid, palmitic acid, or combinations thereof.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of and claims priority to the U.S.patent application Ser. No. 11/849,867 filed on Sep. 4, 2007, publishedas U.S. 2009/0057232A1 and entitled “Composition and Method for RemovingMetal Contaminants,” which is incorporated herein by reference in itsentirety.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not applicable

REFERENCE TO A MICROFICHE APPENDIX

Not applicable

FIELD

The present disclosure relates to compositions and methods for metalremoval. More specifically, the present disclosure relates tocompositions and methods for removal of one or more metal contaminantsfrom a solution.

BACKGROUND

There are a variety of mechanisms by which metal contaminants areintroduced to community resources such as the water supply. Theintroduction of metal contaminants can be attributed to sources such asuntreated waste discharges; discharges of industrial effluent containingchemicals; run-off from agricultural fields containing pesticides; leaksfrom water pipe joints in areas where water pipe and sewage line passclose together; discharges from mining waste and tailings; seepage fromlandfills, or hazardous waste dumps; and corrosion from pipes, fittings,solder, or plumbing. The level of tolerance for such metal contaminantsis low as exposure of an organism to a variety of metals (e.g., heavymetals) at even relatively low concentrations can result in a variety ofadverse effects spanning from both chronic and acute illnesses to thegeneration of water-borne diseases. These effects can be the result ofexposure to high levels of these metals in a single dose or be theresult of the accumulation of these metals in an organism over a longerduration by repeated exposure. Thus, a need exists for an improvedmethod for removing the metal contaminants from liquids.

SUMMARY

Disclosed herein is a method for removing a metal from ametal-containing solution comprising contacting the metal-containingsolution with a metal-removing composition comprising a substrate, anorganic ion, and a metal binding agent, and recovering a solution havinga lowered metal concentration when compared to the metal-containingsolution. The metal-containing solution may comprise a metal, a heavymetal, or combinations thereof. The metal or heavy metal may compriselead, iron, arsenic, mercury, copper, manganese, chromium, barium,cadmium, selenium, antimony, beryllium, nickel, thallium, orcombinations thereof. The metal and/or heavy metal may be present in themetal-containing solution in an amount of equal to or less than about10000 ppm.

The substrate may comprise a natural clay, a synthetic clay, a naturalzeolite, a synthetic zeolite, a polymer resin, lignite, or combinationsthereof. The clay may comprise kaolinite, serpentine, illite, chlorite,smectite or combinations thereof. The smectite may comprisemontmorillonite, saponite, sepiolite, nontronite, beidellite, hectorite,fuller's earth, attapulgite, or combinations thereof. The zeolite maycomprise analcime, chabazite, heulandite, natrolite, phillipsite,stilbite, or combinations thereof. The polymer resin may comprisediethyl aminoethyl, quaternary aminoethyl, or combinations thereof. Thesubstrate may be present in an amount of from about 30% to about 90% byweight of the metal-removing composition.

The organic ion may comprise quaternary amines, imidazolium salts,phosphonium salts, or combinations thereof. The quaternary amines maycomprise tetra alkyl ammonium, bis-(hydrogenatedtallow)-dimethyl-ammonium chloride, bis-(hydrogenatedtallow)-benzyl-methyl-ammonium chloride, or combinations thereof. Theimidazolium salts may comprise4,5-dihydro-1-methyl-2-nortallow-alkyl-1-(2-tallow-amidoethyl)-imidazoliummethyl sulfate,1-ethyl-4,5-dihydro-3-(2-hydroxyethyl)-2-(8-heptadecenyl)-imidazoliumethyl sulfate, or combinations thereof. The organic ion may be presentin an amount of from about 10% to about 70% by weight of the removingcomposition.

The metal-binding agent may comprise a mercaptan, a carboxylic acid, achelating agent, or combinations thereof. The chelating agent maycomprise amines, esters, carboxylic acids, alcohols, ethers, aldehydes,ketones, alkenes, alkynes, mercaptans, thiols, or combinations thereof.The mercaptan may comprise tert-dodecanethiol, nonanethiol, octanethiol,or combinations thereof. The carboxylic acid may comprise n-stearicacid, iso-stearic acid, palmitic acid, or combinations thereof. Themetal-binding agent may comprise an alkyl group comprising from about 2to about 30 carbons. The metal-binding agent may be present in an amountof equal to or less than about 30% by weight of the removingcomposition.

The ratio of the metal-containing solution to the metal-removingcomposition may be about 50:50. The metal-removing composition mayreduce the amount of metal in the metal-containing solution by equal toor greater than about 75%. The metal-containing solution andmetal-removing composition may be contacted for a period of equal to orgreater than about 5 minutes. The method may further comprise separatingthe solution having a lowered metal concentration from themetal-removing composition via filtration, particle filtration, particlesettling, microfiltration, ultrafiltration, nanofiltration, reverseosmosis, centrifuge, screening, or combinations thereof.

Also disclosed herein is a composition comprising a substrate, anorganic ion, and a metal binding agent. The substrate may comprise anatural clay, a synthetic clay, a natural zeolite, a synthetic zeolite,a polymer resin, lignite, or combinations thereof. The clay may comprisekaolinite, serpentine, illite, chlorite, smectite or combinationsthereof. The smectite may comprise montmorillonite, saponite, sepiolite,nontronite, beidellite, hectorite, fuller's earth, attapulgite, orcombinations thereof. The smectite may comprise bentonite. The zeolitemay comprise analcime, chabazite, heulandite, natrolite, phillipsite,stilbite, or combinations thereof. The polymer resin may comprisediethyl aminoethyl, quaternary aminoethyl, or combinations thereof.

The organic ion may comprise quaternary amines, imidazolium salts,phosphonium salts, or combinations thereof. The quaternary amines maycomprise tetra alkyl ammonium, bis-(hydrogenatedtallow)-dimethyl-ammonium chloride, bis-(hydrogenatedtallow)-benzyl-methyl-ammonium chloride, or combinations thereof. Theimidazole salts may comprise4,5-dihydro-1-methyl-2-nortallow-alkyl-1-(2-tallow-amidoethyl)-imidazoliummethyl sulfate,1-ethyl-4,5-dihydro-3-(2-hydroxyethyl)-2-(8-heptadecenyl)-imidazoliumethyl sulfate, or combinations thereof.

The metal-binding agent may comprise mercaptan, carboxylic acid,chelating agents, or combinations thereof. The chelating agent maycomprise, amines, esters, carboxylic acids, alcohols, ethers, aldehydes,ketones, alkenes, alkynes, mercaptans, thiols, and or combinationsthereof. The mercaptan may comprise tert-dodecanethiol, nonanethiol,octanethiol, or combinations thereof. The carboxylic acid may comprisen-stearic acid, iso-stearic acid, palmitic acid, or combinationsthereof. The metal-binding agent may comprise an alkyl group comprisingfrom about 2 to about 30 carbons.

The substrate may be present in an amount of from about 30% to about 90%by weight of the composition. The organic ion may be present in anamount of from about 10% to about 70% by weight of the composition. Themetal-binding agent may be present in an amount of equal to or less thanabout 30% by weight of the composition. The composition may have aneffective functionality to remove metal, heavy metal, or both from asolution.

Further disclosed herein is a composition comprising a substrate, anorganic ion, and a metal-binding agent wherein the organic ion maycomprise a tetraalkyl ammonium salt and the metal-binding agent maycomprise a mercaptan. The substrate may comprise a smectite.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an illustration of a metal-removing composition.

FIG. 2 is a schematic of a process flow diagram.

FIG. 3 is a plot of the amount of arsenic and lead in a metal-containingsolution before and after treatment with a metal removing composition.

FIG. 4 is a plot of the amount of iron in a metal-containing solution asa function of treatment time with a metal-removing composition.

DETAILED DESCRIPTION

While the disclosure is susceptible to various modifications andalternative forms, specific embodiments thereof are shown by way ofexample in the figures and will herein be described in detail. It is tobe understood, however, that the figures and detailed descriptionthereto are not intended to limit the disclosure to the particular formdisclosed, but on the contrary, the disclosure is to cover allmodifications, equivalents and alternatives failing within the spiritand scope of the present disclosure as defined by the appended claims.

Disclosed herein are compositions and methods for removing a metal froma metal-containing solution. In an embodiment, the method comprisescontacting the metal-containing solution with a metal-removingcomposition (MRC) comprising a substrate, an organic ion, and ametal-binding agent.

As disclosed herein, the term “metal-containing solution” (MCS) is meantto include any solution (e.g., aqueous) that comprises at least onemetal, alternatively comprises at least one heavy metal. Heavy metalsrefer to higher atomic weight elements, which have the properties of ametallic substance at room temperature. Examples of such heavy metalsinclude without limitation lead, iron, arsenic, mercury, copper,manganese, chromium, barium, cadmium, selenium, antimony, beryllium,nickel, thallium, or combinations thereof.

In an embodiment, the MCS may comprise aqueous solutions obtained from avariety of sources wherein the aqueous solutions comprise at least oneheavy metal. For example, the MCS may comprise ground water, surfacewater, industrial and/or domestic waste, tap water, or combinationsthereof. In an embodiment, the MCS comprises water produced from asubterranean formation such as for example a wellbore. Heavy metals(e.g. iron, lead) may be present in the untreated MCS in an amount ofequal to or less than about 10,000 parts per million (ppm),alternatively in an amount from about 0.05 ppm to about 5000 ppm, oralternatively in an amount of from about 0.1 ppm to about 1000 ppm. Inanother embodiment, the metal may be present in the untreated MCS in anamount of up to 1000 ppm.

In an embodiment, the MCS may be contacted with a metal-removingcomposition (MRC) wherein the MRC comprises a substrate, an organic ion,and a metal binding agent. An embodiment of a MRC is shown in FIG. 1.Referring to FIG. 1, the MRC 100 comprises a substrate 110 which isassociated with an organic ion 120 which in turn is associated with ametal-binding agent 130. Such compositions may also be referred to asmetal sorbents.

In an embodiment the MRC comprises a substrate. The substrate may be anorganic or an inorganic material. The substrate may be furthercharacterized as hydrophobic, alternatively the substrate ishydrophilic. Examples of materials suitable for use as the substrate inthe MRC include without limitation clay, zeolite, polymeric resin,lignite, or combinations thereof.

In an embodiment, the substrate comprises a clay. Clays herein refer toaggregates of hydrous silicate particles either naturally occurring orsynthetically produced, less than 4 micrometers (μm) in diameter and mayconsist of a variety of minerals rich in silicon and aluminum oxides andhydroxides which include variable amounts of other components such asalkali earth metals and water. Clays are most commonly formed bychemical weathering of silicate-bearing rocks, although some are formedby hydrothermal activity. These clays can be replicated in industrialchemical processes. Examples of clays suitable for use in thisdisclosure include without limitation clays from the following groups:kaolinite, serpentine, illite, chlorite, smectite or combinationsthereof. Example of suitable kaolinite group clays include withoutlimitation kaolinite, dickite, halloysite, nacrite, or combinationsthereof. Examples of suitable illite groups include clay-micas andillite.

In an embodiment, the clay comprises a smectite. Examples of smectitessuitable for use in this disclosure include without limitationmontmorillonite, saponite, sepiolite, nontronite, beidellite, hectorite,fuller's earth, attapulgite or combinations thereof. In anotherembodiment, the smectite comprises a montmorillonite, for example abentonite.

In an embodiment, the substrate comprises a zeolite. Zeolites arethree-dimensional, microporous, crystalline solids with well-definedporous structures. Zeolites, which can be either naturally occurring orsynthesized, comprise a group of hydrated alumina silicates that arelinked in a three dimensional framework through shared oxygen atoms.Examples of zeolites suitable for use in this disclosure include withoutlimitation analcime, chabazite, heulandite, natrolite, phillipsite,stilbite, or combinations thereof.

In an embodiment, the substrate comprises a polymeric resin such as forexample an ion-exchange resin. Ion exchange resins are polymeric resinsthat contain charged functional groups. The base polymer is usually acrosslinked material such as polystyrene that is crosslinked with avinyl polymer. Examples of polymeric resins suitable for use in thisdisclosure include without limitation diethyl aminoethyl, quaternaryaminoethyl, Mono-Q, Mono-S, or combinations thereof, all of which arecommercially available from Pharmacia Biotech.

In an embodiment, the substrate comprises a lignite. Lignite is abrownish black coal that has high inherent moisture content and high ashcontent compared to bituminous coal. It is a heterogenous mixture andoften has a woodlike texture. Lignite may have a heat content rangingfrom about 10 MJ/kg to about 20 MJ/kg.

In some embodiments, the substrate may be obtained from natural sources,alternatively the substrate may comprise synthetic analogs of thematerials described herein. Such synthetic analogs and methods ofpreparing same are known to one of ordinary skill in the art.

In an embodiment, the substrate may be present in amount of from about30% to about 90%, alternatively from about 65% to about 85%, oralternatively from about 70% to about 80% by weight of the MRC.

In an embodiment, the MRC comprises an organic ion. The organic ion mayinclude any positively charged organic molecule. In some embodiments,the organic ion may be an oil wetting agent, a bactericide, orcombinations thereof. For example, the organic ion may comprise aquaternary amine, imidazolium salt, phosphonium salt, or combinationsthereof. Examples of suitable quaternary amines include withoutlimitation tetra alkyl ammonium, bis-(hydrogenatedtallow)-dimethyl-ammonium chloride, bis-(hydrogenatedtallow)-benzyl-methyl-ammonium chloride, or combinations thereof.Examples of suitable imidazolium salts include without limitation4,5-dihydro-1-methyl-2-nortallow-alkyl-1-(2-tallow-amidoethyl)-imidazoliummethyl sulfate,1-ethyl-4,5-dihydro-3-(2-hydroxyethyl)-2-(8-heptadecenyl)-imidazoliumethyl sulfate.

In an embodiment, the organic ion is present in an amount of from about10% to about 70%, alternatively from about 15% to about 35%, oralternatively from about 25% to about 30% by weight of the MRC.

In an embodiment, the MRC comprises a metal-binding agent. Themetal-binding agent may function to bind and remove the metals from theMCS. In an embodiment, the metal-binding agent comprises at least onemetal-binding functional group and a hydrophobic group.

In an embodiment, the metal-binding functional group comprises amercaptan. Mercaptans, also known as thiols, are sulfur-containingorganic compounds comprising the functionality generally represented as[—SH]. Examples of suitable mercaptans include without limitationtert-dodecanethiol, nonanethiol, octanethiol, or combinations thereof.In an embodiment, the thiol may comprise from 6 to 30 carbon atoms.

In an embodiment, the metal-binding functional group comprises acarboxylic acid. A carboxylic acid is an organic acid characterized bythe presence of a carboxyl group which is represented as [—C(═O)OH].Examples of carboxylic acids suitable for use in this disclosure includewithout limitation n-stearic acid, iso-stearic acid, palmitic acid, orcombinations thereof.

In an embodiment, the metal binding agent may have both mercaptan andcarboxylic acid functionalities. Alternatively the metal-binding agentcomprises a compound such as a chelating agent (also termed coordinatingagent) having a plurality of metal-binding functionalities. Chelatingagents generally refer to compounds having the ability to coordinate ametal through more than one bond. For example, a chelating agent mayhave one mercaptan group and one carboxylic acid group, alternativelytwo mercaptan groups and two carboxylic acid groups. Alternatively, thechelating agent may comprise amines, esters, carboxylic acids, alcohols,ethers, aldehydes, ketones, alkenes, alkynes, mercaptans, thiols, orcombinations thereof.

In an embodiment, the metal-binding agent comprises a hydrophobic groupwhich is bonded to the metal-binding functionality (e.g. mercaptan,carboxylic acid, chelating agent) and may be any hydrophobic groupcompatible with the metal-binding agent and the other components of theMRC. In an embodiment, the hydrophobic group comprises an alkyl grouphaving n carbon atoms wherein n is from about 2 to about 30,alternatively from about 5 to about 25, alternatively from about 10 toabout 20. The hydrophobic group may be chosen (e.g. length of the alkylchain) to meet the needs of the process and overall may function toincrease the hydrophobicity of the MRC. Without wishing to be limited bytheory, the substrate which may initially be hydrophilic, afterassociation with an organic ion and/or the metal-binding agent having ahydrophobic group may display an increased degree of hydrophobicity.Alternatively, the substrate chosen may be hydrophobic in nature and thehydrophobicity of the substrate would again be increased by associationof the substrate with the metal-binding agent and/or the organic ion.The degree of hydrophobicity can be adjusted by one skilled in the artby adjusting the nature of the hydrophobic group (e.g. length of thealkyl chain).

In an embodiment, the metal-binding agent is present in an amount ofequal to or less than about 30%, or alternatively equal to or less thanabout 10%, or alternatively equal to or less than about 5% by weight ofthe MRC.

The amounts of all components of the MRC presented herein are by way ofexample. It is to be understood these amounts may be adjustedaccordingly by one of ordinary skill in the art using the benefit of thepresent disclosure in order to prepare a composition that functionswithin the spirit and scope defined herein.

The MRC may be prepared by contacting the substrate with the organicion, where both the substrate and organic ions are solids, to form asolid mixture. Alternatively, the MRC may be prepared by contacting thesubstrate with an organic ion where the substrate is a solid while theorganic ion is a liquid to form a solid-liquid mixture. The solid orsolid-liquid mixture can be agitated to achieve a blended mixture by anymeans known to one of ordinary skill in the art. For example the solidmixture can be crushed with a mortar and pestle, and then agitated usingan agitator or an ultrasonic mixer. In some embodiments, a solid-liquidmixture comprising the substrate, and organic ion may be blended andsubsequently dried in an oven, or alternatively in a vacuum oven to forma dried mixture. The solid or the dried mixture can be further contactedwith a metal-binding agent where the metal-binding agent is provided aseither a solid or a liquid. The components may be mixed as previouslydescribed herein and may be contacted and blended in a fashion similarto that described for the contacting and blending of the organic ion andsubstrate. Additionally, process condition such as temperature,pressure, time, and the like may be adjusted as desired by one ofordinary skill in the art to meet the needs of the process.

An embodiment of a process flow diagram for preparing the MRC isschematized in FIG. 2. Referring to FIG. 2, the process 200 comprises asubstrate feed 210 and an organic ion feed 215 to a first mixer 220. Allor a portion of the feed streams (e.g., feeds 210 and 215) to theprocess may be combined prior to reaching the mixers (e.g., mixer 220).The mixed composition from the first mixer is passed via flowline 225 toa second mixer 235. A metal binding agent feed 230 is added to theflowline 240, and/or may optionally be added at other locations in theprocess such as to mixer 220, mixer 235, or both. The MRC may exit themixer 235 via flowline 240.

In an embodiment the MRC may be prepared by contacting the substrate,the organic ion, and the metal binding agent in any order desired by theuser and, compatible with the components of the mixture. For example,with reference to FIG. 2, a method of preparing an MRC may compriseintroducing substrate feed 210 to mixer 220, followed by the organic ionfeed 215, and then the metal binding agent feed 230, as depicted in FIG.2. Alternatively, the organic ion 215 may comprise the initial feed,followed by the substrate feed 210, and then the metal binding agentfeed 230. In an embodiment, the MRC components may be fed throughindependent feedlines into mixers 220 mixer 230 where the MRC componentsmay be combined. Alternatively, the components may be premixed in afeedline before entering the mixer where they may be further contacted.In an embodiment, two of the components may be premixed and/or stored inseparate storage units, and premixed in a mixing unit before being feedto mixers 230. The premixing may be designed to produce certaincharacteristics (e.g. homogeneity) and as such the premixing conditions(e.g., time period, agitation methods) may be chosen by one of ordinaryskill in the art to meet the needs of the process. The mixers may be ofany type known in the art and compatible with the disclosed process suchas for example agitators or extruders. In an embodiment, the mixer is anextruder.

In an embodiment, a method of reducing the amount of metal in a MCScomprises contacting the MCS with an MRC of the type described herein.The MCS may be contacted with the MRC using any method known to one ofordinary skill in the art. The contacting may occur in a contactingzone. As used herein, the term contacting zone refers to any vessel,container, or unit wherein a user desired process occurs and wherein theprocess may comprise any number and/or type of interactions between itscomponents (e.g. physical, chemical, etc. . . . ). In an embodiment, thecontacting may be further assisted by agitation to achieve a blendedmixture. In some embodiments, the MRC may a component of a fixed bedwhich is contacted with the MCS by flow of the MCS over the fixed bed.In such embodiments, additional conditions such as the flow rate of theMCS and the dimensions of the fixed bed may be chosen by one of ordinaryskill in the art to meet the needs of the process. In an embodiment, theMCS and MRC may be contacted at a ratio of MCS:MRC of about 50:50,alternatively about 95:5, or alternatively about 99:1.

The contacting time may be varied to achieve a user desired result. Inan embodiment, the contacting time may be equal to or greater than about5 minutes, alternatively from about 5 to about 60 minutes oralternatively from about 15 to about 20 minutes.

In an embodiment, the contacting of the MCS and MRC may result in asolution having a metal content which is reduced in comparison to theMCS and is hereafter referred to as a solution having a lowered metalconcentration (SLMC). In an embodiment, the method of reducing theamount of metal in a MCS may further comprise separating the SLMC fromthe MRC. Separation of the SLMC from the MRC may be accomplished by anymeans known to one of ordinary skill in the art for the separation ofthese type of compositions. For example, these compositions may beseparated using techniques such as filtration, centrifugation,screening, particle settling, or combinations thereof. In an embodiment,the SLMC is separated from the MRC by filtration. Examples of suitablefiltration methods include without limitation particle filtration,microfiltration, ultrafiltration, nanofiltration, and reverse osmosis.

In some embodiments, the SLMC once separated from the MRC may beintroduced to another MRC to further reduce the metal concentration inthe solution. For example, the SLMC may be introduced to a fresh MRCthat has not been previously contacted with a MCS and result in theremoval of at least a portion of any metal remaining in the SLMC.

In an embodiment, the contacting of the MRC and MCS and separation ofthe SLMC from the MRC may be carried out in a preexisting systemcompatible with such processes. For example, the MRC may be a componentof a filter and may function as a component of a system designed toreduce contaminants in a solution. In some embodiments, such systemswhich comprise one or more contact zones comprising components for theremoval of metals from an MCS may have an MRC introduced as anadditional component to the system. Alternatively, at least a portion ofthe components of a preexisting system for the removal of metal from anMCS may be replaced by an MRC of the type disclosed herein. Examples ofsuch systems include without limitation systems designed for waterfiltration, water purification, organic solvent filtration, glycerinpurification, methanol purification, and oil based purification.

After the MRC has contacted the MCS and reduced the concentration ofmetal therein, the resulting mixture, hereinafter termed the spent MRC,may be disposed of; alternatively the spent MRC may be regenerated suchas to produce an MRC that is capable of reacting with a MCS and reducingthe metal concentration of the MCS. Methods of regenerating the spentMRC following exposure to the MCS may be carried out using any methodknown to one of ordinary skill in the art. For example, regeneration canbe achieved by contacting (i.e. mixing, agitating, stirring) the spentMRC with a hydrophobic solvent such as hexanes, dichloromethane, orpetroleum ether to produce a hydrophobic solution containing the metalbound to the metal binding agent (SMM) and a substrate/organic ion solidmixture (SO). The SMM and the SO may be separated by any method known toone of ordinary skill in the art for the separation of suchcompositions. The SO may then be reactivated by contacting it with ametal binding agent of the type and in the manner described herein.

The compositions and methods disclosed herein may result in a reductionin the metal content of the MCS of equal to or greater than about 75,80, 85, 90, 95, 96, 97, 98, 99, or 100%.

EXAMPLES

The invention having been generally described, the following examplesare given as particular embodiments of the invention and to demonstratethe practice and advantages thereof. It is understood that the examplesare given by way of illustration and are not intended to limit thespecification or the claims to follow in any manner.

Example 1

An MRC was prepared by mixing 61.6 g of bentonite (commerciallyavailable from BPM) with 48.7 g of bis-(hydrogenatedtallow)-dimethyl-ammonium chloride. The mixture was blended and crushedwith a mortar and pestle. Next, 40 ml of distilled water was added, andmixed for 30 minutes to form a blended slurry. The blended slurry wasdried in an oven at 75° C. overnight. The dried mixture was then crushedusing the mortar and pestle to a fine powder and weighted at 92.6 g.Next, 4.63 g of ter-dodecanethiol (5% w/w) was added to the fine powder,and mixed to achieve a well-blended mixture for 15 minutes. Next, 30 mlof distilled water was added, mixed for another 20 minutes, and dried inan oven at 75° C. for 12 hours to form the MRC.

The removal of arsenic from an MCS containing arsenic was investigated.An MCS (50 ml) containing 110 ppm arsenic was placed in a beaker. Next,1 g of the MRC prepared as described above was added into the beaker.The mixture was agitated to achieve a blended mixture. The finalsolution was analyzed for arsenic concentration by Induced Couple Plasma(ICP). FIG. 3A is a bar graph depicting the initial and the finalarsenic concentration in the MCS treated with the MRC. The resultdemonstrates that after the treatment, the arsenic concentration levelwas below the detection limit of the ICP, which was below 0.008 ppm

Example 2

The removal of lead from an MCS containing lead was investigated. TheMRC prepared in Example 1 was used to treat an MCS containing 83 ppmlead. After the treatment, the lead concentration was analyzed by ICPand found to be 16 ppm. FIG. 3B is a bar graph depicting the initial andfinal lead concentration in the MCS treated with the MRC.

Example 3

The removal of iron from an MCS containing iron was investigated. TheMRC prepared in Example 1 was contacted with an MCS containing 2 ppmiron for about 60 minutes. The concentration of iron in the MCS wasanalyzed by ICP several times periodically within the 60 minute period.FIG. 4 is a plot of the exposure time against the iron concentration inthe MCS. As observed in FIG. 4, the longer the exposure time, the lowerthe iron concentration in the MCS.

Example 4

The removal of multiple heavy metals from an MCS containing iron, lead,and arsenic was investigated. The MRC prepared in Example 1 was used totreat an MCS containing 110 ppm iron, 33.2 ppm lead, and 11 ppm arsenic.After exposure to the MRC, the final concentration of iron, lead, andarsenic was analyzed by ICP and found to be less than 0.002 ppm (belowthe detection limit of ICP), less than 0.006 ppm (below the detectionlimit of ICP), and 0.02 ppm respectively.

While embodiments of the invention have been shown and described,modifications thereof can be made by one skilled in the art withoutdeparting from the spirit and teachings of the invention. Theembodiments described herein are exemplary only, and are not intended tobe limiting. Many variations and modifications of the inventiondisclosed herein are possible and are within the scope of the invention.Where numerical ranges or limitations are expressly stated, such expressranges or limitations should be understood to include iterative rangesor limitations of like magnitude falling within the expressly statedranges or limitations (e.g., from about 1 to about 10 includes, 2, 3, 4,etc.; greater than 0.10 includes 0.11, 0.12, 0.13, etc.). For example,whenever a numerical range with a lower limit, R_(L), and an upperlimit, R_(U), is disclosed, any number falling within the range isspecifically disclosed. In particular, the following numbers within therange are specifically disclosed: R═R_(L)+k*(R_(U)−R_(L)), wherein k isa variable ranging from 1 percent to 100 percent with a 1 percentincrement, i.e., k is 1 percent, 2 percent, 3 percent, 4 percent, 5percent, . . . 50 percent, 51 percent, 52 percent, . . . , 95 percent,96 percent, 97 percent, 98 percent, 99 percent, or 100 percent.Moreover, any numerical range defined by two R numbers as defined in theabove is also specifically disclosed. Use of the term “optionally” withrespect to any element of a claim is intended to mean that the subjectelement is required, or alternatively, is not required. Bothalternatives are intended to be within the scope of the claim. Use ofbroader terms such as comprises, includes, having, etc. should beunderstood to provide support for narrower terms such as consisting of,consisting essentially of, comprised substantially of, etc.

Accordingly, the scope of protection is not limited by the descriptionset out above but is only limited by the claims which follow, that scopeincluding all equivalents of the subject matter of the claims. Each andevery claim is incorporated into the specification as an embodiment ofthe present invention. Thus, the claims are a further description andare an addition to the embodiments of the present invention. Thediscussion of a reference in the Description of Related Art is not anadmission that it is prior art to the present invention, especially anyreference that may have a publication date after the priority date ofthis application. The disclosures of all patents, patent applications,and publications cited herein are hereby incorporated by reference, tothe extent that they provide exemplary, procedural or other detailssupplementary to those set forth herein.

What is claimed is:
 1. A composition comprising: a substrate, an organicion, and a metal binding agent, wherein the substrate comprisesbentonite in an amount of from about 30% to about 90% by weight of thecomposition; wherein the organic ion comprises bis-(hydrogenatedtallow)-benzyl-methyl-ammonium chloride in an amount of from about 10%to about 70% by weight of the composition; and wherein the metal-bindingagent comprises tert-dodecanethiol and iso-stearic acid in an amount ofequal to or less than about 30% by weight of the composition.
 2. Amixture comprising the composition of claim 1 and a metal selected fromthe group consisting of lead, iron, arsenic, mercury, copper, manganese,chromium, barium, cadmium, selenium, antimony, beryllium, nickel,thallium, and combinations thereof.
 3. A mixture comprising thecomposition of claim 1 and a metal or heavy metal.
 4. A mixturecomprising the composition of claim 1 and a metal-containing solution.5. The mixture of claim 4 wherein the metal-containing solution is anaqueous solution and the metal therein is selected from the groupconsisting of lead, iron arsenic, mercury, copper, manganese, chromium,barium, cadmium, selenium, antimony, beryllium, nickel, thallium, andcombinations thereof.
 6. The composition of claim 1, further comprisinga metal-containing solution, wherein the metal-containing solution is anaqueous solution and the metal therein is selected from the groupconsisting of lead, iron, arsenic, mercury, copper, manganese, chromium,barium, cadmium, selenium, antimony, beryllium, nickel, thallium, andcombinations thereof.
 7. A composition comprising: a substrate,comprising at least one smectite selected from the group consisting ofmontmorillonite, saponite, sepiolite, nontronite, beidellite, hectorite,fuller's earth, and attapulgite, an organic ion, and a metal-bindingagent, wherein the organic ion comprises at least one tetraalkylammonium salt selected from the group consisting of bis-(hydrogenatedtallow)-dimethyl-ammonium chloride, and bis-(hydrogenatedtallow)-benzyl-methyl-ammonium chloride and the metal-binding agentcomprises a compound, wherein the compound comprises at least onemercaptan group selected from the group consisting oftert-dodecanethiol, nonanethiol, and octanethiol and a carboxylic acidgroup.
 8. The composition of claim 7 wherein: the substrate is presentin an amount of from about 30% to about 90% by weight of thecomposition; the organic ion is present in an amount of from about 10%to about 70% by weight of the composition; and the metal-binding agentis present in an amount of equal to or less than about 30% by weight ofthe composition.
 9. A mixture comprising the composition of claim 7 anda heavy metal.
 10. A mixture comprising the composition of claim 7 and ametal selected from the group consisting of lead, iron, arsenic,mercury, copper, manganese, chromium, barium, cadmium, selenium,antimony, beryllium, nickel, thallium, and combinations thereof.
 11. Themixture of claim 10 wherein the metal is a component of ametal-containing solution.
 12. A composition comprising a substratecomprising a smectite wherein the smectite comprises bentonite, anorganic ion, and a metal-binding agent, wherein the organic ioncomprises a tetraalkyl ammonium salt comprising bis-(hydrogenatedtallow)-dimethyl-ammonium chloride and the metal-binding agent comprisesa compound, wherein the compound comprises a mercaptan group comprisingtert-dodecanethiol and a carboxylic acid group.
 13. The composition ofclaim 12 wherein: the substrate is present in an amount of from about30% to about 90% by weight of the composition; the organic ion ispresent in an amount of from about 10% to about 70% by weight of thecomposition; and the metal-binding agent is present in an amount ofequal to or less than about 30% by weight of the composition.
 14. Amixture comprising the composition of claim 12 and a metal wherein themetal is selected from the group consisting of lead, iron, and arsenic.